Associated Papers
Dominant frontonasal dysplasia with ectodermal defects results from increased activity of ALX4.
Peled A et al.
American Journal of Medical Genetics. Part A, 2023
De novo ALX4 variant detected in child with non-syndromic craniosynostosis.
Fonteles CS et al.
Brazilian Journal of Medical and Biological Research = Revista Brasileira De Pesquisas Medicas E Biologica, 2021
Variants in ALX4 and their association with genitourinary defects.
Chen CH et al.
Andrology, 2020
A Novel Missense Variant in the ALX4 Gene Underlies Mild to Severe Frontonasal Dysplasia in a Consanguineous Family.
Hussain S et al.
Genetic Testing and Molecular Biomarkers, 2020
Closing the Gap: Genetic and Genomic Continuum from Syndromic to Nonsyndromic Craniosynostoses.
Heuzé Y et al.
Current Genetic Medicine Reports, 2014
Genetic analysis of the role of Alx4 in the coordination of lower body and external genitalia formation.
Matsumaru D et al.
European Journal of Human Genetics : Ejhg, 2014
ALX4 gain-of-function mutations in nonsyndromic craniosynostosis.
Yagnik G et al.
Human Mutation, 2012
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